A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5598



Internal ID9627304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:143427140..143594148hg38UCSC Ensembl
Innerchr4:144348293..144515301hg19UCSC Ensembl
Innerchr4:144567743..144734751hg18UCSC Ensembl
Innerchr4:144705898..144872906hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg38167009
hg19167009
hg18167009
hg17167009
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2757960
Supporting Variants
SamplesNA18529
Known GenesFREM3, GAB1, GUSBP5, SMARCA5, SMARCA5-AS1
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv5598
Frequency
Sample Size270
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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